Refsum Disease, Classic,Agnosia,Spinocerebellar Ataxia Type 1 With Axonal Neuropathy,Pontocerebellar Hypoplasia, Type 7,Spastic Ataxia, Charlevoix-Saguenay Type,Mitochondrial Dna Depletion Syndrome 7,Motor Peripheral Neuropathy,Oculomotor Apraxia,Choreatic Disease,Cerebellar Disease,Tay-Sachs Disease,Ataxia-Oculomotor Apraxia 3,Dystonia,Prostate Squamous Cell Carcinoma,Neuropathy,Peripheral Nervous System Disease,Cardiofaciocutaneous Syndrome 1,Vestibular Nystagmus,Ataxia With Vitamin 3 Deficiency,Autosomal Dominant Cerebellar Ataxia,Xeroderma Pigmentosum, Variant Type,Friedreich Ataxia,Disease Of Mental Health,Achalasia-Addisonianism-Alacrima Syndrome,Multiple Acyl-Coa Dehydrogenase Deficiency,Dentatorubral-Pallidoluysian Atrophy,Mental Retardation, X-Linked, With Cerebellar Hypoplasia And Distinctive Facial Appearance,Spinocerebellar Ataxia 14,Spinocerebellar Ataxia, Autosomal Recessive, With Axonal Neuropathy 2,Coenzyme Q10 Deficiency, Primary, 4,Coenzyme Q10 Deficiency Disease,Lig4 Syndrome,Marinesco-Sjogren Syndrome,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Spastic Ataxia,Spastic Paraplegia 7, Autosomal Recessive,Coenzyme Q10 Deficiency, Primary, 1,Apraxia,Charcot-Marie-Tooth Disease, Axonal, Type 2cc,Ataxia-Telangiectasia,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Kearns-Sayre Syndrome,Ocular Motor Apraxia

Seizure Disorder,Neuromuscular Disease,Corpus Callosum, Agenesis Of,Intellectual Disability - Hypoplastic Corpus Callosum - Preauricular Tag,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Neuromuscular Oculoauditory Syndrome,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome

Hepatocellular Carcinoma

Cerebellar Disease,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Seckel Syndrome,Riddle Syndrome,Lig4 Syndrome,Renal Cell Carcinoma, Nonpapillary,Nijmegen Breakage Syndrome,Ataxia-Telangiectasia,Primary Autosomal Recessive Microcephaly

Epilepsy,Benign Epilepsy With Centrotemporal Spikes,Psychomotor Retardation, Epilepsy, And Craniofacial Dysmorphism

Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Riddle Syndrome

Skin Melanoma,Cervical Intraepithelial Neoplasia,Neuroendocrine Tumor,Endometrial Cancer,Squamous Cell Carcinoma,Clear Cell Meningioma,Malignant Fibrous Histiocytoma,Endometrial Hyperplasia,Desmoid Tumor,Adenoma,Myxofibrosarcoma,Parathyroid Carcinoma,Adenosarcoma,Mucoepidermoid Carcinoma,Benign Meningioma,B-Cell Lymphoma,Oral Leukoplakia,Sinonasal Undifferentiated Carcinoma,Embryonal Sarcoma,Keratocystic Odontogenic Tumor,Brain Ependymoma,Congenital Mesoblastic Nephroma,Polymorphous Low-Grade Adenocarcinoma,Cavernous Hemangioma,Pulmonary Vein Stenosis,Leiomyoma,Basal Cell Carcinoma,Necrotizing Sialometaplasia,Transitional Cell Carcinoma,Bladder Cancer,Soft Tissue Sarcoma,Spitz Nevus,Leukoplakia,Breast Ductal Carcinoma,Breast Cancer,Colorectal Cancer,Hepatocellular Carcinoma,Ameloblastic Carcinoma,Keratoacanthoma,Inverted Papilloma,Spinal Cord Melanoma,Central Neurocytoma,Bowen'S Disease,Breast Disease,Prostate Cancer,Papillary Thyroid Microcarcinoma,Epithelioid Trophoblastic Tumor,Adrenal Cortical Carcinoma,Breast Fibroadenoma,Bladder Adenocarcinoma,Cervical Squamous Cell Carcinoma,Sarcoma, Synovial,Barrett Esophagus,Gastrointestinal Stromal Tumor,Inflammatory Myofibroblastic Tumor,Renal Cell Carcinoma, Nonpapillary,Meningioma, Familial,Ductal Carcinoma In Situ,Lung Cancer

Laminopathy,Bare Lymphocyte Syndrome, Type I,Glycerol Kinase Deficiency